Stent-graft having facing side branch portals

ABSTRACT

In various embodiments, a device for treating disease of a vessel includes a stent graft having an outer surface; and at least two side branch portals each having a proximal end and a distal end. Each distal end is substantially contiguous with the outer surface of the stent graft. In various other embodiments, the distal ends are generally axially further spaced apart than the proximal ends.

BACKGROUND

1. Field

The present disclosure relates to stent grafts for treating disease ofthe vasculature.

2. Discussion of the Related Art

Disease of the vasculature is increasingly common and, because of thetortuous nature and complexity of the vasculature, is difficult formedical practitioners to treat. By way of example, aortic dissectionscommonly begin at or near the aortic valve root and continue to theascending aorta and the aortic arch, and may also affect the upper partof the descending aorta. The three branch vessels off the aortic arch,namely, the brachiocephalic artery and the left common carotid and leftsubclavian arteries, are anatomically difficult for medicalpractitioners to access and ultimately treat effectively.

Disease of the vasculature is currently treated surgically (e.g., openrepair, endovascular repair, or a hybrid of the two). Surgicalapproaches to aortic arch repair known in the art include elephant trunkrepair and the trifurcated graft technique. However, existing approachesoften are highly invasive and/or require specially designed grafts.

There is thus a need in the art for improved, less invasive, andsimplified devices, systems and methods for treating disease of thevasculature.

SUMMARY

In various embodiments, devices, systems and methods for treatingdisease of the vasculature, such as the ascending aorta, aortic arch,and descending aorta, are disclosed. In various embodiments, a stentgraft is provided with at least two side branch portals, each having aproximal end and a distal end. The side branch portal's distal end iscontiguous with the outer surface of the stent graft. In variousembodiments, a side branch portal has an elbow configuration such thatits proximal end can be oriented antegrade/retrograde within the stentgraft. In yet other various embodiments, a side branch portal has aT-shaped configuration such that its proximal end is split and can beoriented antegrade/retrograde. In various embodiment, one or more sidebranch portals having a T-shaped configuration are located between outerside branch portals having elbow configurations. In various embodiments,a stent graft comprises side branch portals having elbow configurationswith proximal ends facing each other (e.g., antegrade/retrograde). Invarious embodiments, the distal ends of the side branch portals aregenerally axially further spaced apart than the proximal ends.

An exemplary system comprises a stent graft having at least two sidebranch portals as described above, crush loaded, retained by orotherwise housed within a sleeve with a tubular element passing throughthe side branch portals, so as to preserve a pathway for a branch wire.In an embodiment, the proximal and distal ends of the tubular elementextend away from the stent graft through distinct slits in the sleeve.In accordance with an aspect of an embodiment, the distal end of thetubular element is closed.

Another exemplary system comprises a stent graft having at least twoside branch portals as described above, together with one or more sidebranch stent grafts and/or one or more extenders installed at a proximalend of the stent graft.

In accordance with an exemplary method, a stent graft having at leasttwo side branch portals is crush loaded, retained by or otherwise housedwithin a sleeve and delivered along a guidewire to a treatment location.Once in position, the stent graft may be deployed and side branch stentgrafts may be installed at side branch portals.

In exemplary embodiments using a stent graft comprising side branchportals having elbow configurations with proximal ends facing eachother, the stent graft may be crush loaded with a tubular elementpassing through the side branch portals, so as to preserve a pathway fora branch wire. Thereafter, the stent (crush loaded into a sleeve) isdelivered along a guidewire to a treatment location, the stent isdeployed, and side branch stent grafts can be passed along the branchwire and installed at side branch portals. One or more extenders may beinstalled at a proximal end of the stent graft as needed.

BRIEF DESCRIPTION OF THE DRAWINGS

The features and advantages of the present disclosure will become moreapparent from the detailed description set forth below when taken inconjunction with the drawings.

FIG. 1 a illustrates a top view of an exemplary stent graft comprisingside branch portals having elbow configurations with proximal endsfacing each other, aligned on a single or parallel plane.

FIG. 1 b illustrates a front view cross section of FIG. 1 a.

FIG. 1 c illustrates a top view of an exemplary stent graft comprising aside branch portal having a T-shaped configuration located between outerside branch portals having elbow configurations.

FIG. 1 d illustrates a front view cross section FIG. 1 c.

FIG. 2 a illustrates a branch wire threaded through exemplary sidebranch portals having elbow configurations with proximal ends facingeach other.

FIG. 2 b illustrates an exemplary delivery configuration wherein thestent graft is crush loaded with a tubular element passing through theside branch portals.

FIG. 3 illustrates exemplary aortic arch bypass configurations.

FIG. 4 illustrates a method comprising a guidewire and a branch wire inaccordance with an exemplary embodiment.

FIG. 5 a illustrates a crush loaded stent graft at a treatment locationin accordance with an exemplary embodiment.

FIG. 5 b illustrates a deployed stent graft with side branch stentgrafts at a treatment location in accordance with an exemplaryembodiment.

FIG. 6 a illustrates an exemplary mono-branch.

FIG. 6 b illustrates an exemplary aneurysmal extender.

FIG. 6 c illustrates an exemplary coronary extender.

DETAILED DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS

Persons skilled in the art will readily appreciate that various aspectsof the present invention may be realized by any number of methods andapparatuses configured to perform the intended functions. Stateddifferently, other methods and apparatuses may be incorporated herein toperform the intended functions. It should also be noted that theaccompanying drawing figures referred to herein are not all drawn toscale, but may be exaggerated to illustrate various aspects of thepresent invention, and in that regard, the drawing figures should not beconstrued as limiting. Finally, although the present invention may bedescribed in connection with various principles and beliefs, the presentinvention should not be bound by theory.

In accordance with exemplary embodiments, the present invention providesfor improved, less invasive, and simplified devices, systems and methodsfor treating disease of the vasculature. Exemplary embodiments enablebranch-to-branch placement of a branch wire, which greatly simplifiesplacement of side branch stent grafts for installation at side branchportals of a larger stent graft.

The invention will be described primarily with reference to treatingdisease of the ascending aorta, aortic arch, and descending aorta,however, the invention may be applied to other disease of thevasculature, including, for example, any disease where a larger vesseland one or more branch vessels are to be treated.

With reference to FIGS. 1 a-1 b, a stent graft 100, in accordance withvarious embodiments, has at least two side branch portals 110. In itsexpanded configuration, an exemplary stent graft diameter may beapproximately the same as the vessel to be repaired. In anotherembodiment, the expanded stent graft diameter may be slightly largerthan the vessel to be treated to provide a traction fit within thevessel. Similarly, an exemplary expanded side branch portal diameter maybe approximately the same as the vessel to be repaired. Preferably, thecross section is circular, but other cross sections may be suitableincluding but not limited to profiles that are “D” shaped, oval,triangular, square, polygon shaped or randomly shaped.

The stent graft and side branch portals may comprise materials now knownin the art or later discovered, for example, a nitinol helical or ringstructure and one or more ePTFE coverings (e.g., one or more coatings onthe luminal and/or abluminal surfaces). FIG. 1 a, for instance, depictsa stent graft comprising a plurality of zig-zag rings 103 along thelength of the stent graft 100, and having ePTFE coverings 105 on theluminal and abluminal surfaces. Other useful materials may comprisenylons, polycarbonates, polyethylenes, polypropylenes,polytetrafluoroethylenes, polyvinyl chlorides, polyurethanes,polysiloxanes, stainless steels, or other biocompatible materials.

The stent graft and side branch portals may be comprised of the same ordifferent materials and may be coupled together as a modular element bynow known or as yet unknown methods, for example, by an interferencefit, adhesives, sutures, clips or the like. In another embodiment, thestent graft and side branch portals are integrally formed.

In exemplary embodiments, a side branch portal comprises a proximal end112 and a distal end 114. In exemplary embodiments, a side branchportal's distal end 114 is substantially contiguous with the outersurface of the stent graft 100, while in other embodiment a distal end114 extends laterally outward from the outer surface of the stent graft100. Distal ends in exemplary embodiments may be spaced apart, forinstance, depending on the spacing between the branch vessels to betreated. A stent graft may comprise two or more side branch portals, andthe center points of some or all of their distal ends 114 may be alignedalong a single axis that is generally parallel with the longitudinalaxis of the stent graft. In other embodiments, with reference to FIG. 1a, a plurality of distal ends 114 of side branch portals 110 are offset,for example, by a distance equal to, or greater than the diameter of theside branch portals themselves at their distal ends (or the largest sidebranch portal distal end if sized differently).

In exemplary embodiments, and as best seen in FIG. 1 b, a side branchportal has an elbow configuration 116 such that its proximal end 112 canbe oriented completely or partially antegrade or retrograde within thestent graft 100. Indeed, the inventors have surprisingly found thatretrograde perfusion may be at least as effective as antegradeperfusion.

While an “elbow configuration” may correspond to an angle ofapproximately 90 degrees, larger and smaller angles are alsocontemplated for use with the present invention. In some embodiments, aside branch portal 110 is not angled; stated differently, the centerpoints of its proximal and distal ends are aligned along a common axis,for example, an axis that is generally perpendicular to the longitudinalaxis of the stent graft.

Turning to FIGS. 1 c-1 d, in yet other exemplary embodiments, a sidebranch portal 110 has a bifurcated configuration (e.g., a T-shapedconfiguration 118) such that its proximal end 112 is split and can beoriented completely or partially antegrade and retrograde. Stateddifferently, proximal end 112 may have a plurality of distinct openings,for example, a first opening oriented completely or partially antegradeand a second opening oriented completely or partially antegraderetrograde. Again, angles larger and smaller than approximately 180degrees are contemplated, but in an exemplary embodiment, the anglebetween proximal ends is approximately 180 degrees (i.e., the proximalends face in opposite directions). In one embodiment, one or moreunangled side branch portals 110 and/or side branch portals 110 having aT-shaped configuration 118 are located between outer side branch portals110 having elbow configurations 116.

In a preferred embodiment, a stent graft comprises side branch portalshaving elbow configurations with proximal ends aligned on a parallel,common or substantially similar plane, facing each other (e.g., oneantegrade and the other retrograde, one at an angle relative toantegrade flow and the other at the corresponding angle relative toretrograde flow). Importantly, proximal ends in exemplary embodimentsmay be spaced apart, for instance, depending on the spacing between thebranch vessels to be treated.

Moreover, while the center points of proximal ends may be aligned alonga single axis that is generally parallel with the longitudinal axis ofthe stent graft, proximal ends in exemplary embodiments may be offset,for example, by a distance equal to, or greater than the diameter of theside branch portals themselves at their proximal ends (or the largestside branch portal proximal end if sized differently). By way ofillustrations, a side branch portal includes a longitudinal axisextending through the center point of its proximal end. In variousembodiments, the longitudinal axes of the side branch portals are notco-axial. In other embodiments, the longitudinal axes of the side branchportals are substantially parallel. In yet other embodiments, thelongitudinal axes of the side branch portals are generally parallel witha longitudinal axis of the stent graft. In still other embodiments, thelongitudinal axes of the side branch portals are generally aligned alonga common plane. In accordance with exemplary embodiments, the distalends are generally axially further spaced apart than the proximal ends.In yet other embodiments, longitudinal axes of side branch portals areskewed in relation to each other and/or the longitudinal axis of thestent graft.

In various embodiments, the proximal ends may be aligned on a commonplane, or on parallel or angled planes, such that a generally clearpathway exists through the portals' proximal ends. It should beunderstood that the pathway need not be parallel with the longitudinalaxis of the stent graft. In an embodiment, one or more side branchportals having a T-shaped configuration are interposed between sidebranch portals having elbow configurations. In such an embodiment, thepathway through the portals' proximal ends need not be linear.

An exemplary system comprises a stent graft having at least two sidebranch portals as described above, crush loaded or otherwise collapsedover a tubular element and, retained by or otherwise housed within asleeve.

The term “tubular element” includes any longitudinally extendingstructure with or without a through lumen. Thus, tubular elementsinclude but are not limited to tubes with lumens, solid rods, hollow orsolid wires (e.g., guidewires), hollow or solid stylets, metal tubes(e.g., hypotubes), polymer tubes, pull cords or tethers, fibers,filaments, electrical conductors, radiopaque elements, radioactiveelements and radiographic elements. Tubular elements can be of anymaterial and can have any cross-sectional shape including but notlimited to profiles that are circular, oval, triangular, square, polygonshaped or randomly shaped.

The sleeve may be comprised of one or more of nylons, polycarbonates,polyethylenes, polypropylenes, polytetrafluoroethylenes, polyvinylchlorides, polyurethanes, polysiloxanes, stainless steels, or otherbiocompatible materials. In yet other embodiments, the sleeve is atubular element.

Making reference to FIGS. 2 a-2 b, in exemplary embodiments, a stentgraft 200 is crush loaded and constrained by a constraining sleeve 240with one or more tubular elements 220 passing through some or all of theside branch portals 210, so as to preserve a conduit there through(e.g., a pathway for a branch wire 230). Stated differently, a lumenthrough some or all of the side branch portals 210 may be preservedwhich guides a guidewire while the stent graft 200 remains constrainedby the constraining sleeve 240. In this embodiment, the tubular element220 may be threaded (passed through) in the distal end 214 and out theproximal end 212 of one side branch portal 210 and in the proximal end212 and out the distal end 214 of another side branch portal 210. Insome embodiments, the tubular element is additionally threaded throughproximal ends of one or more side branch portals having a T-shapedconfiguration.

In an embodiment, the proximal end 222 and distal ends 224 of a tubularelement 220 extend out opposite distal ends of the side branch portalsand away from the stent graft through the sleeve 240. Passage throughthe sleeve may be accomplished by various configurations including butnot limited to one or more slits 242, holes, windows, voids, etc. in thesleeve suitable for passage of the tubular element. In an embodiment,the alignment of the slit 242 is selected to prevent tearing of thesleeve 240. Passage may also be accomplished through a plurality ofsleeves, for example, a central sleeve and two lateral sleeves. Here,the proximal end 222 and distal ends 224 of a tubular element 220 extendout opposite distal ends of the side branch portals generally at thejunctions between the central sleeve and two lateral sleeves.

In accordance with an aspect of an embodiment, the distal end 224 of thetubular element 220 is closed to block passage of an inner tubularelement (e.g., a guidewire). Limiting advancement of the inner tubularelement through the side branch portals in this manner may facilitateremoval of the tubular element 220 from the constrained stent graft. Thedistal end may be closed in various embodiments by heat sealing, or byusing an end cap, plug or the like, shown for illustration purposes asreference numeral 226.

Other exemplary systems comprise a stent graft having at least two sidebranch portals as described above, together with one or more side branchstent grafts and/or one or more extenders installed at a proximal end ofthe stent graft. Exemplary side branch stent grafts may be independentor connected to each other, as will be discussed below. Exemplaryextenders include aneurysmal and coronary extenders, as will also bediscussed below.

Exemplary methods for use in connection with the devices and systemswill now be described, however, they should not be construed as limitingthe scope of the present invention, but rather as illustrative.

In accordance with one exemplary method, a guidewire is tracked from ananatomical access (e.g., a fenestration or opening in an artery or vein)through the vasculature to an anchoring location, located distal to atreatment location, using now known or as yet unknown techniques. Thedistal end of the guidewire is then anchored at the anchoring location,again, using now known or as yet unknown methods, such as a ballooncatheter.

Next, a stent graft having at least two side branch portals, asdescribed herein, is crush loaded or otherwise collapsed over a tubularelement and, retained by or otherwise housed within a sleeve, anddelivered along the guidewire to the treatment location.

Optimal positioning of the stent graft may be determined by various nowknown or as yet unknown techniques. By way of example, radiopaquemarkers or indicators can be incorporated into the stent graft, sidebranch portals or the tubular element(s) to facilitate placement andvisualization within the vasculature. Fluoroscopic visualization,contrast injection and/or other technologies known in the art may alsobe used to assist in positioning of the stent graft.

Once in position, the stent graft is deployed by removing the sleeve,after which one or more side branch stent grafts may be installed atside branch portals, typically through the side branch(es) to betreated.

Exemplary methods for treating disease of the ascending aorta, aorticarch, and descending aorta will now be described. With reference to FIG.3, an ascending aorta 370, aortic arch 375, and descending aorta 380 areshown. With continued reference to FIG. 3, a medical practitioner maydiagnose disease of the brachiocephalic artery 350 or the left commoncarotid artery 355 or left subclavian artery 360. The practitioner mayperform a single bypass 365 or double bypass 365 and may desire todeploy a stent graft in the aortic arch 375 and treat each of thedisease free branch vessels off the aortic arch with a side branchportal.

Turning to FIG. 4, in accordance with one exemplary method, a guidewire435 is tracked from an incision in the femoral artery through the aortato the left ventrical using now known or as yet unknown techniques. Thedistal end of the guidewire 435 is then anchored within the leftventrical, again, using now known or as yet unknown methods, such as aballoon catheter.

A branch wire 430 is then tracked from an incision in a branch vessel tobe treated (the brachiocephalic artery 450 in FIG. 4) through the aortato the incision in the femoral artery using now known or as yet unknowntechniques. More than one branch wire 430 may be used, for example, inconnection with a stent graft comprising one or more side branch portalshaving a T-shaped configuration located between outer side branchportals having elbow configurations. In this manner, more than twobranch vessels may be treated.

Next, a stent graft having at least two side branch portals(corresponding to the two disease free branch vessels off the aorticarch), as described herein, is crush loaded or otherwise collapsed overa tubular element and, retained by or otherwise housed within a sleeve440. In various embodiments and as described above, the side branchportals have proximal ends aligned on a parallel, common orsubstantially similar plane, facing each other. The proximal and/ordistal ends of the side branch portals may or may not be offset, asdiscussed above.

The stent graft is crush loaded with a tubular element passing throughthe side branch portals, so as to preserve a pathway for the branch wirethrough the side branch portals. In embodiments comprising one or moreside branch portals having a T-shaped configuration located betweenouter side branch portals having elbow configurations, more than onetubular element may passing through the stent graft and side branchportals, so as to preserve multiple pathways for multiple branch wiresthrough the side branch portals. The proximal and distal ends of thetubular element(s) extend out distal ends of the side branch portals andaway from the stent graft through a slit in the sleeve.

As the crush loaded stent graft is delivered along the guidewire to theaortic arch, the branch wire 430 is threaded through the side branchportals via the tubular element. In some embodiments, the distal end ofthe tubular element may be capped such that the tubular element ispushed completely out of the side branch portals and stent graft uponthreading of the branch wire.

With reference to FIGS. 5 a-5 b, the stent graft 500 is thus deliveredto the aortic arch 575 in its compressed configuration. As describedabove, optimal positioning of the stent graft may be determined byvarious now known or as yet unknown techniques.

Once optimally positioned, the end of the branch wire 530 extending intothe femoral artery can be snared out another branch vessel to be treated(the left subclavian artery 560 in FIG. 5 a). A loop snare may be usedfor this purpose, or any other snare method now known in the art orlater discovered. In embodiments having more than one tubular elementand more than one branch wire for the treatment of more than two branchvessels, similar snaring techniques may be used to snare the end of eachbranch wire 530 extending into the femoral artery out the particularbranch vessel to be treated.

Traction is optionally applied to the ends of the branch wire(s) toposition the stent graft so it is “snug” along the outer curvature ofthe aortic arch 575.

Turning to FIG. 5 b, in exemplary embodiment, the stent graft is thendeployed by removing the sleeve. Sleeve removal may be accomplished byvarious now known or as yet unknown methods, such as a pull cordextending through the femoral access. In an embodiment, the stent graftmay be deployed by simply unstitching the sleeve. Stated differently, itmay not be necessary to remove the sleeve in an embodiment.

Finally, one or more side branch stent grafts 590 may be installed atside branch portals 510 of stent graft 500. With momentary reference toFIG. 6 a, in one embodiment, a plurality of side branch stent grafts 590are interconnected to each other, for example, by a bridge 695.

Turning back to FIG. 5 a-5 b in exemplary embodiments, side branch stentgrafts 590 are passed along the branch wire 530 through the side branchvessels 550 ad 560 to be treated. With reference to FIG. 5 b, care maybe taken so that a side branch stent graft 590 does not extend beyond abypass graft 591. A side branch stent graft 590 may be crush loaded orotherwise collapsed over a tubular element and, retained by or otherwisehoused within a sleeve. Side branch stent grafts 590 may be coupled atside branch portals by now known or as yet unknown methods, for example,by an interference fit, adhesives, sutures, clips or the like.

One or more extenders may be installed at a proximal and/or distal endof the stent graft as needed. In general, an extender may extend thestent graft closer to the aortic valve root and beyond, for example, tothe coronary arteries. Similar to a stent graft within the spirit andscope of the invention, an extender may be comprised of materials nowknown in the art or later discovered, for example, a nitinol helical orring structure and one or more ePTFE coverings. Other useful materialsmay comprise nylons, polycarbonates, polyethylenes, polypropylenes,polytetrafluoroethylenes, polyvinyl chlorides, polyurethanes,polysiloxanes, stainless steels, or other biocompatible materials.

Extenders may be coupled to the stent graft prior to insertion oradvanced along the guidewire through the lumen of the stent graftsubsequent to its radial deployment. Exemplary extenders includeaneurysmal and coronary extenders, as shown in FIGS. 6 b and 6 c,respectively.

An exemplary aneurysmal extender may comprise a radial stiff portion 692and a radial compliant portion 693 having an increasing, frustoconicalstyle diameter, and being configured to seal with minimum force.

An exemplary coronary extender may comprise one inside the other. Anexemplary coronary extender may comprise one or more side branch stentgrafts 694 to be installed in one or more coronary arteries. Inembodiments comprising a coronary extender, a guidewire may be insertedinto the coronary arteries to guide placement of the extender.

It will be apparent to those skilled in the art that variousmodifications and variations can be made in the present inventionwithout departing from the spirit or scope of the invention. Thus, it isintended that the present invention cover the modifications andvariations of this invention provided they come within the scope of theappended claims and their equivalents.

What is claimed is:
 1. A system for treating vascular disease, saidsystem comprising: a catheter; a stent graft having at least a pair ofside branch portals, each of the pair of side branch portals having twoends, with one end being substantially contiguous with the outer surfaceof the stent graft; the stent graft constrained onto a catheter forendoluminal delivery of the stent graft; and a guidewire tube thatextends through each pair of side branch portals and preserves a lumenwhich guides a guidewire through each pair of side branch portals whilethe stent graft remains constrained by the constraining sleeve, whereinan end of the guidewire tube is closed to limit advancement of theguidewire therethrough while the guidewire tube extends through eachpair of side branch portals of the constrained stent graft.
 2. Thesystem as set forth in claim 1, wherein the guidewire tube is removableafter the guidewire is received therethrough.
 3. The system as set forthin claim 1, wherein opposite ends of the guidewire tube extend away fromthe stent graft through distinct slits in the constraining sleeve. 4.The system as set forth in claim 1, further comprising one or more sidebranch stent grafts installed at each pair of side branch portals. 5.The system as set forth in claim 1 further comprising at least one sidebranch stent graft extending through at least one of the side branchportals for treating a branch vessel.
 6. The system as set forth inclaim 1 further comprising at least two side branch stent graftsextending respectively through each pair of side branch portals.
 7. Thesystem as set forth in claim 6, wherein two of the at least two sidebranch stent grafts are interconnected.
 8. The system as set forth inclaim 1, further comprising an extender installed at a proximal end ofthe stent graft.
 10. The device as set forth in claim 1, wherein eachside branch portal includes a longitudinal axis extending through thecenter point of its respective proximal end.
 11. The device as set forthin claim 10, wherein the longitudinal axes of each of the pair of sidebranch portals are generally aligned along a common plane.
 12. Thedevice as set forth in claim 10, wherein the longitudinal axes of eachof the pair of side branch portals are not co-axial.
 13. The device asset forth in claim 12, wherein the longitudinal axes of the side branchportals are substantially parallel.
 14. The device as set forth in claim12, wherein the longitudinal axes of the side branch portals aregenerally parallel with a longitudinal axis of the stent graft.
 15. Thedevice as set forth in claim 1, wherein each side branch portal pairincludes a first end that is substantially contiguous with the outersurface of the stent graft and an opposite second end, the second end ofone of the pair of side branch portals faces antegrade.
 16. The deviceas set forth in claim 1, wherein each side branch portal pair includes afirst end that is substantially contiguous with the outer surface of thestent graft and an opposite second end, the second end of one of thepair of side branch portals faces retrograde.
 17. The device as setforth in claim 1, wherein each side branch portal pair includes a firstend that is substantially contiguous with the outer surface of the stentgraft and an opposite second end, the second end of one of the pair ofside branch portals faces antegrade and the second end of the other ofthe pair of side branch portals faces retrograde.
 18. The device as setforth in claim 1, wherein at least one of the pair of side branchportals comprises a bifurcated configuration.
 19. The device as setforth in claim 18, wherein the side branch portal having the bifurcatedconfiguration is generally T-shaped.
 20. The device as set forth inclaim 1 including a third side branch portal having a T-shapedconfiguration and being disposed between the pair of side branchportals.
 21. The device as set forth in claim 20, wherein each pair ofside branch portals are generally elbow-shaped.
 22. The device as setforth in claim 1, wherein at least one side branch portal is generallyelbow-shaped.
 23. The device as set forth in claim 1 including aconstraining sleeve for constraining the stent graft onto the catheterfor endoluminal delivery of the stent graft, wherein opposite ends ofthe guidewire tube extend outside of the constraining sleeve.
 24. Amethod of assembling a system for treating vascular disease, said methodcomprising: providing a catheter; providing a stent graft having atleast a pair of side branch portals, each of the pair of side branchportals having two ends, with one end being substantially contiguouswith the outer surface of the stent graft; constraining the stent graftwith a constraining sleeve on an end of the catheter for endoluminaldelivery of the stent graft; providing a guidewire tube, wherein an endof the guidewire tube is closed to limit advancement of the guidewiretherethrough while the guidewire tube extends through each pair of sidebranch portals of the constrained stent graft; and extending theguidewire tube through each pair of side branch portals and therebypreserving a lumen for guiding a guidewire through each pair of sidebranch portals while the stent graft remains constrained by theconstraining sleeve.